Evidence map›Paper›PMID 28446566›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2017

Induction of Adaptive Immunity Leads to Nigrostriatal Disease Progression in MPTP Mouse Model of Parkinson's Disease.

Goutam Chandra, Avik Roy, Suresh B Rangasamy, Kalipada Pahan

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 2 pooled it
3.5field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 2 syntheses or guidelines pooled it, 61 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Goutam ChandraDepartment of Neurological Sciences, Rush University Medical Center, Chicago, IL 60612; and.
Avik RoyDepartment of Neurological Sciences, Rush University Medical Center, Chicago, IL 60612; and.ORCID 0000-0003-0523-8504
Suresh B RangasamyDepartment of Neurological Sciences, Rush University Medical Center, Chicago, IL 60612; and.ORCID 0000-0003-4867-1551
Kalipada PahanDepartment of Neurological Sciences, Rush University Medical Center, Chicago, IL 60612; and Kalipada_Pahan@rush.edu.
Rush University Medical Center · US

Funding

RANTES and Eotaxin: New players in PD progressionR01NS083054 · NINDS · RUSH UNIVERSITY MEDICAL CENTER · PI PAHAN, KALIPADA · 2013 to 2017
$1.7M
Cinnamon and its metabolite sodium benzoate in ParkinsonismI01BX003033 · VA · JESSE BROWN VA MEDICAL CENTER · PI PAHAN, KALIPADA · 2016 to 2020
–
BLRD VA I01 BX003033NINDS NIH HHS R01 NS083054
6 · The paper itself

Abstract

Although the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) mouse model is the most widely used animal model for Parkinson's disease (PD), it is known that nigrostriatal pathologies do not persist in the acute MPTP mouse model. This study highlights the importance of adaptive immunity in driving persistent and progressive disease in acute MPTP-intoxicated mice. Although marked infiltration of T cells into the nigra was found on 1 d of MPTP insult, T cell infiltration decreased afterward, becoming normal on 30 d of insult. Interestingly, twice-weekly supplementation of RANTES and eotaxin, chemokines that are involved in T cell trafficking, drove continuous T cell infiltration to the nigra and incessant glial inflammation. Supplementation of RANTES and eotaxin was also associated with the induction of nigral α-synuclein pathology, persistent loss of dopaminergic neurons and striatal neurotransmitters, and continuous impairment of motor functions in MPTP-intoxicated mice. In contrast, supplementation of TNF-α and IL-1β, widely studied proinflammatory cytokines, did not induce persistent disease in MPTP-insulted mice. Our results suggest that induction of adaptive immunity by RANTES and eotaxin could hold the key for driving persistent nigrostriatal pathologies in the MPTP mouse model, and that targeting these factors may halt disease progression in PD patients.

Indexed as

Adaptive ImmunityAcute DiseaseAnimalsChemokine CCL11Chemokine CCL5Disease ProgressionInflammationInterleukin-1betaMiceMice, Inbred C57BLMPTP PoisoningSubstantia NigraTumor Necrosis Factor-alphaCcl11 protein, mouseCcl5 protein, mouseChemokine CCL11Chemokine CCL5Interleukin-1betaTumor Necrosis Factor-alpha

Identifiers

PMID28446566
PMCPMC5467696
OpenAlexW2611573935

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.